A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909587



Internal ID22684797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9370038..9385219hg38UCSC Ensembl
chr8:9227548..9242729hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3815182
hg1915182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17447498
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909587
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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